Publications by authors named "Er-Chi Zhou"

Article Synopsis
  • S-DNA is a specialized form of DNA that forms under high tension and is resistant to cleavage by certain enzymes like Cas12a and restriction endonucleases.* -
  • The researchers developed an assay using magnetic tweezers that allows for the separation of single-DNA molecules from multiple-DNA-tethered beads, enabling precise cleavage of only those that do not transition to S-DNA.* -
  • This innovative method enhances the accuracy of measuring DNA properties and cleavage rates, reducing errors often encountered in experiments involving multiple-DNA-tethered beads.*
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The detection of nucleic acid sequences in parallel with the discrimination of single nucleotide variations (SNVs) is critical for research and clinical applications. A few limitations make the detection technically challenging, such as too small variation in probe-hybridization energy caused by SNVs, the non-specific amplification of false nucleic acid fragments and the few options of dyes limited by spectral overlaps. To circumvent these limitations, we developed a single-molecule nucleic acid detection assay without amplification or fluorescence termed THREF (hybridization-induced tandem DNA hairpin refolding failure) based on multiplexed magnetic tweezers.

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As a key dsDNA recognition receptor, cyclic guanosine monophosphate (GMP)-AMP synthase (cGAS) plays a vital role in innate immune responses. Activated cGAS, by sensing DNA, catalyzes the synthesis of the secondary messenger cyclic GMP-AMP (cGAMP), which subsequently activates downstream signaling to induce production of interferons and inflammatory cytokines. Here, we report Zyg-11 family member B (ZYG11B) as a potent amplifier in cGAS-mediated immune responses.

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CpG methylation of DNA is common in mammalian cells. In sperm, the DNA has the highest level of CpG methylation and is condensed into toroidal structures. How CpG methylation affects DNA structures and interactions is important to understand its biological roles but is largely unknown.

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Article Synopsis
  • Most single-molecule manipulation configurations for DNA and RNA involve multiple single-stranded strands with functional labels at both ends for surface attachment.
  • We developed a new amplification-annealing (AA) assay that simplifies the creation of various DNA/RNA configurations in just two or three steps, avoiding complex digestion and ligation processes.
  • These configurations can be used in advanced manipulation techniques like optical tweezers, magnetic tweezers, and atomic force microscopy, as well as other surface-tethering methods.
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S-DNA (stretched DNA) is an elongated base-paired DNA conformation under high tension. Because the RecA/Rad51 family DNA recombinases form helical filaments on DNA and mediate the formation of the DNA triplex (D-loop), in which the DNA is stretched, and because the extension of these nucleoprotein filaments is similar to the extension of S-DNA, S-DNA has long been hypothesized as a possible state of DNA that participants in RecA/Rad51-mediated DNA strand exchange in homologous recombination. Such a hypothesis, however, is still lacking direct experimental studies.

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